Actively Recruiting
Solarplast (R) Supplementation Effects Following High-intensity Resistance Exercise
Led by Kent State University · Updated on 2024-05-29
46
Participants Needed
1
Research Sites
49 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The primary goal of this investigation is to assess whether Solarplast (R) supplementation will improve recovery following heavy resistance exercise in active adults. The primary questions to be addressed are: Does Solarplast (R) decrease muscle damage and inflammation associated with heavy resistance exercise? Does Solarplast (R) reduce the decline in performance associate with heavy resistance exercise? Researchers will compare Solarplast (R) to a placebo (a look-alike substance that contains no active ingredients) to see if Solarplast (R) is effective at improving recovery. Participants will be asked to: Take Solarplast (R) or placebo daily for 4 weeks Visit the laboratory at least once per week to receive their supplement Report to the lab for 3 consecutive visits following supplementation to complete a heavy resistance training session and follow-up testing.
CONDITIONS
Official Title
Solarplast (R) Supplementation Effects Following High-intensity Resistance Exercise
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Recreationally active, participating in at least 2 weight training workouts per week over the past year and at least 3 hours of structured exercise per week
- Judged healthy and free of physical limitations by the investigator
- Body mass index between 18.0 and 34.9 kg/m2, inclusive
- Willing to maintain habitual diet throughout the study
- Willing to abstain from dietary supplementation during the study
- Understands study procedures and provides informed consent
You will not qualify if you...
- Currently enrolled or planning to enroll in another clinical trial
- Habitual consumer of green or black tea over 8 oz/day within 14 days prior to screening
- History or presence of significant cardiac, renal, hepatic, endocrine (including diabetes), pulmonary, biliary, gastrointestinal, pancreatic, or neurologic disorders
- History or presence of cancer in the prior 2 years except non-melanoma skin cancer
- Unable to perform physical exercise
- Engaged in extreme diets such as Atkins, South Beach, or Intermittent Fasting
- Allergic to the study product or placebo
- Taking any nutritional supplements or performance enhancing drugs
- Has chronic illness requiring continuous medical care
- Taking any prescription or over-the-counter medications including corticosteroids, NSAIDs, or antibiotics within 14 days prior to screening
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Kent State University - Exercise Science & Exercise Physiology
Kent, Ohio, United States, 44242
Actively Recruiting
Research Team
A
Adam R Jajtner, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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